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NCT Number: NCT07262580

The Feasibility of an Intervention Targeting Sources of Meaning in Cardiac Rehabilitation

Being diagnosed with heart disease can be a life-changing experience, often sparking existential questions and concerns about meaning in life. A lack of meaning in life has been found associated with increased emotional distress and decreased quality of life. Health professionals recognize that issues related to personal meaning in life are relevant but rarely address these aspects systematically in cardiac rehabilitation. This may be due to a lack of necessary tools.

The project evaluates a novel, brief and structured intervention that aims to strengthen the experience of meaningfulness and reduce or prevent emotional distress by addressing personal sources of meaning in life among patients attending cardiac rehabilitation and their relatives in Denmark. The intervention is based on the Sources of Meaning Card Method, a method developed by Peter la Cour and Tatjana Schnell to map and explore personal sources of meaning (www.somecam.org). For the current project, the method has been adapted for a cardiac rehabilitation context.

Three intervention formats are examined in a feasibility study in a municipal rehabilitation setting: 1) an individual format for patients in cardiac rehabilitation, 2) a dyadic format including a patient together with a relative, and 3) a group format for patients. Approximately 60 patients and 20 relatives are expected to participate. The study explores (a) participants' experience with and acceptability of the intervention formats; (b) changes in meaningfulness and emotional distress in a pre-post design; (c) recruitment and adherence rate, and (d) acceptability and practicality of the three formats among rehabilitation professionals.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Sundhed og Forebyggelse, Odense, Region Syddanmark, Denmark

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

A.

Inclusion criteria

, individual and group-based intervention formats:

  • ≥18 years of age
  • attending municipal cardiac rehabilitation
  • proficiency in Danish

Exclusion criteria

, individual and group-based intervention formats:

  • severe psychiatric disorder
  • severe cognitive impairment

B. Inclusion criteria, patients in dyadic intervention format

  • as in A
  • and having a relative who would like to participate

Inclusion criteria

, relative in dyadic intervention format:

  • ≥18 years of age
  • relative to a patient attending municipal cardiac rehabilitation
  • proficiency in Danish

Exclusion criteria

, patient and relative dyadic intervention format

  • as in A

Treatment and study plan

Conversation on Sources of Meaning in life with heart disease

Other

The intervention uses the brief and structured Sources of Meaning Card Method (SoMeCaM; www.somecam.org), which has been adapted for use in cardiac rehabilitation. It explores personal sources of meaning in a conversation with one patient in a 1-hour session. It comprises 26 cards each including statements on a particular source of meaning. The patient prioritizes the cards, reflects on them, and identifies possibilities for change.

The conversation is facilitated by a professional (trained master students in psychology) and followed up with a phone call approximately 4 weeks after the conversation.

Group based session on Sources of Meaning in life with heart disease

Other

The intervention is based on the brief and structured Sources of Meaning Card Method (SoMeCaM; www.somecam.org), which has been adapted for use in groups in a cardiac rehabilitation context. The method uses 26 cards, each representing a specific source of meaning. Approximately 6-10 participants are guided through a process of individually prioritizing the cards, reflecting on them and identifying potential areas for change or development in smaller groups. The group-based format enables mutual sharing and support in reflection and change processes among patients.

The workshop is facilitated by a professional (trained master students in psychology) and followed up with individual phone calls with all participants approximately 4 weeks after the conversation.

Dyadic Conversation on Sources of Meaning in Life with heart disease

Other

The intervention is based on the brief and structured Sources of Meaning Card Method (SoMeCaM; www.somecam.org), which has been adapted for use in dyads in a cardiac rehabilitation context. The method uses 26 cards, each representing a specific source of meaning. The dyadic format considers both the patient's and the relative's individual and shared sources of meaning in 1 session, which may enhance understanding for each other's sources of meaning and facilitate their joint daily life. They both prioritize the cards individually, reflect on them and identify possibilities for change through a talk-and-listen approach.

The conversation is facilitated by a professional (trained master students in psychology) and followed up with a phone call approximately 4 weeks after the conversation.

Primary outcomes

  1. Participants' experiences with the three intervention formats

    Time frame: Approximately 1 month post intervention

    Defined as the participants' experiences with their participation in one of the three intervention formats. Explored via focus groups and semi structured interviews.

  2. Theoretical Framework of Acceptability (TFA) Questionnaire

    Time frame: 1 month post intervention

    Participants' acceptability of the intervention will be quantitatively assessed using the Theoretical Framework of Acceptability (TFA) Questionnaire. This scale evaluates the following seven constructs: affective attitude, burden, ethicality, opportunity costs, perceived effectiveness, self-efficacy, and intervention coherence.

    Each item is rated on a 5-point Likert scale ranging from 1 to 5. Higher scores indicate greater acceptability of the intervention across the measured domains.

  3. Acceptability of the three intervention formats among participants

    Time frame: Approximately 1 month post intervention

    Acceptability will be explored qualitatively via focus groups and semi-structured interviews with participants enrolled in one of the three intervention formats

  4. Changes in symptoms of depression

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    The Patient Health Questionnaire 9-item depression scale (PHQ-9) will be used to assess symptoms of depression in the past two weeks. Each item is scored 0 to 3. The severity score can range from 0 to 27, with higher scores indicating more severe symptoms.

  5. Changes in symptoms of anxiety

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    The 7-item General Anxiety Disorder Scale (GAD-7) will be used to measure symptoms of anxiety in the past two weeks. Each item is scored 0 to 3, providing a 0 to 21 severity score, with higher scores indicating more severe symptoms.

  6. Changes related to meaning in life

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    Changes in participants' self-reported experience of meaning in life will be assessed using two validated subscales from the Sources of Meaning and Meaning in Life Questionnaire: the Meaningfulness and Crisis of Meaning subscales.

    Each subscale consists of 5 items, scored on a Likert scale from 0 (Strongly disagree) to 5 (Strongly agree).

    For the Meaningfulness subscale, higher scores indicate a stronger sense of meaning in life.

    For the Crisis of Meaning subscale, higher scores indicate a stronger experience of life as empty, pointless and lacking of meaning.

  7. Recruitment rate

    Time frame: From study start until recruitment ends (approximately 1 year)

    Recruitment rate is defined as the proportion of participants who consented to participate in the study, reported as a percentage over the recruitment period.

  8. Intervention adherence

    Time frame: Through study completion, approximately 1 year

    The proportion of participants who completed the full intervention, defined as participation in the one-session Sources of Meaning conversation (individual, patient-relative, or group-based) and the follow-up phone call. Data will be recorded by the research team.

  9. Study attrition (dropout rate)

    Time frame: Through study completion (approximately 15 months from study start)

    The proportion of participants who drop out from the study before completing all parts of the intervention, the 3 surveys and focus group and/or individual interview. Dropout will be assessed via administrative data.

  10. Acceptability among rehabilitation professionals

    Time frame: After study enrollment (approximately 1 year from study start)

    Acceptability of the three intervention formats will be explored via focus groups with rehabilitation professionals involved in cardiac rehabilitation. The focus groups will address professionals' views on the interventions and perceived usefulness of the intervention in the municipal cardiac rehabilitation setting.

  11. Practicality of the intervention formats among rehabilitation professionals

    Time frame: After study enrollment (approximately 1 year from study start)

    Defined as the rehabilitation professionals' evaluation of whether the intervention can be successfully used in practice (municipal cardiac rehabilitation). Including factors such as time, resources, and workflow compatibility. Explored via focus group with professionals in the municipal cardiac rehabilitation.

  12. Intervention facilitators' experience with delivering the intervention

    Time frame: Through study completion (approximately 1 year from study start)

    Intervention facilitators will document their experience using semi-structured worksheets with field notes completed after each intervention session. These will capture reflections on feasibility, participant responsiveness, and challenges encountered in each step of the intervention.

Secondary outcomes

  1. Changes in health-related quality of life

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    Explores changes in participants' self-reported health-related quality of life measured by EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5L).

    The EQ-5D-5L consists of 2 scales: the descriptive system (EQ-5D) and the EQ visual analogue scale (EQ VAS).

    EQ-5D measures the five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each with 5 levels from 'no problems', 'slight problems', 'moderate problems', 'severe problems' to 'extreme problems'.

    EQ VAS captures the participant's self-rated health on a vertical visual scale from 0-100 where 100 means: 'The best health you can imagine' and 0 means 'The worst health you can imagine'.

    Higher scores indicate better self-reported health-related quality of life.

  2. Changes in awareness on sources of meaning in everyday life.

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    Changes in awareness on sources of meaning in everyday life will be explored using a purpose-designed self-report measure with 2 items covering awareness rated on a Likert scale ranging from 0 (Strongly disagree) to 5 (Strongly agree). Higher scores indicate greater awareness on sources of meaning in everyday life.

  3. Changes in engagement in sources of meaning in everyday life

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    Changes in engagement in sources of meaning in everyday life will be explored using purpose-designed self-report measure with 3 items covering engagement rated on a Likert scale ranging from 0 (Strongly disagree) to 5 (Strongly agree). Higher scores indicate greater engagement on sources of meaning

  4. Changes in mutual understanding (dyadic intervention arm)

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    Mutual understanding between patients and relatives in the dyadic intervention format will be assessed using the Understanding Subscale of the Perceived Partner Responsiveness Scale (PPRS) (Reis & Carmichael, 2006).

    The subscale consists of 5 items rated on a 9-point Likert scale ranging from 1 (Not at all true) to 9 (Very true). Higher scores indicate higher mutual understanding in the relationship to the other person.

  5. Changes in relationship quality (dyadic intervention arm)

    Time frame: Baseline, 1 month post intervention and 3 months post intervention

    Relationship quality will be assessed using the Relationship Ladder, a single-item visual analogue scale in which participants rate their perceived relationship quality on a scale from 0 (Very poor) to 10 (Excellent).

    Higher scores indicate better perceived relationship quality.

  6. Intervention costs

    Time frame: Through study completion (approximately 1 year post study start)

    To calculate intervention costs, information on time spent by intervention facilitators and other staff as well as material costs will be collected.

  7. Reasons for dropout

    Time frame: At time of dropout (Up to 4 months post intervention)

    Reasons for participant dropout will be collected using a voluntary purpose-designed 3-item questionnaire at the time of dropout.

  8. Engagement in intervention

    Time frame: 1 month post intervention

    Participant's engagement in the intervention is assessed through 2 purpose-designed questions: (1) 'Thought about the conversation at home' and (2) 'Used the reflection booklet at home'. Each question has an option to elaborate the answer qualitatively.

Sponsors and collaborators

Lead sponsor

University of Southern Denmark

Other

Collaborators

  • Danish Heart Foundation
  • Odense Municipality, Denmark

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Dec 3, 2025
Registry last updated
Jan 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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